GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances errors or problems from a medical device for example. GMP is also sometimes referred to as “cGMP”. the “c” stands for “current,” reminding manufacturers that they must employ technologies and systems which are up-to-date in order to comply with the regulation. Systems and equipment used to prevent errors or failure in a medical device for example. Because of GMP guidelines are not prescriptive instructions on how to manufacture products, so GMP should be updated according to FDA Quality Regulations.